Revisiting Skull Metastases of Prostate Cancer at Prostate-Specific Membrane Antigen (PSMA) Positron Emission Tomography/Computed Tomography Era: PSMA Uptake Characteristics and Oncological Outcomes.

0 UROLOGY & NEPHROLOGY
Baris Esen, Okan Falay, Kayhan Tarim, Hulya Seymen, Mert Kilic, Sevil Bavbek, Yakup Kordan, Mehmet Onur Demirkol, Derya Tilki, Tarik Esen
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Abstract

Objective: We aimed to evaluate prostate-specific membrane antigen (PSMA) uptake characteristics and the oncological outcomes in patients with skull metastases.

Methods: The records of 345 serial PSMA positron emission tomography (PET)/computed tomography (CT) scans of 96 patients with metastatic prostate cancer (PCa) were evaluated retrospectively. Skull bone metastasis was detected in 18 patients (18/96, 18.7%), with a mean age of 72.4 ± 9.1 years, and in 40 PSMA PET/CT scans (40/345, 11.6%). Involved skull bones, PSMA uptake characteristics, and CT counterparts of metastatic lesions were centrally reviewed. Prostate specific antigen (PSA) levels at the time of skull metastasis detection and PSMA-detected other metastatic lesions were recorded.

Results: All patients with a skull metastasis showed multiple other metastatic bone lesions, and 6 (33.3%) had visceral metastasis. Seven (38.9%) patients had solitary skull lesions, whereas 11 (61.1%) had multiple skull metastases. Twenty-two out of 37 (59.5%) metastatic lesions had no CT counterpart. The median SUVmax was significantly higher in metastatic lesions with a CT counterpart (median 9.09 vs. 4.63, P = .018). At a median follow-up of 23.4 mo (interquartile range [IQR] 8.7-34.1) after detection of skull metastasis, 5 out of 11 (45.5%) hormone-sensitive and all castration-resistant patients died of PCa. The median survival of patients with castration-resistant disease was 9.92 months.

Conclusion: The majority of PSMA-detected skull metastases did not show a CT counterpart, which may explain why skull metastases were rarely detected before the PSMA PET-era. In high-volume metastatic prostatic cancer cases, 68Ga-PSMA PET/CT imaging field including the vertex, may enhance the accuracy in detecting tumor extent and metabolic tumor volume.

在前列腺特异性膜抗原(PSMA)正电子发射断层扫描/计算机断层扫描时代重访前列腺癌颅骨转移:PSMA摄取特征和肿瘤预后。
目的:探讨前列腺特异性膜抗原(PSMA)在颅内转移瘤患者中的摄取特点及预后。方法:回顾性分析96例转移性前列腺癌(PCa)患者的345例PSMA正电子发射断层扫描(PET)/计算机断层扫描(CT)记录。颅骨转移18例(18/96,18.7%),平均年龄72.4±9.1岁,PSMA PET/CT扫描40例(40/345,11.6%)。受累颅骨、PSMA摄取特征和转移性病变的CT对应物被集中回顾。记录头颅转移检测时的前列腺特异性抗原(PSA)水平以及其他转移灶的PSA检测水平。结果:所有颅骨转移患者均有多发性骨转移灶,其中6例(33.3%)有内脏转移。7例(38.9%)患者有单发颅骨病变,11例(61.1%)患者有多发颅骨转移。37例转移灶中有22例(59.5%)未见CT对应灶。与CT相对应的转移性病变中位SUVmax明显更高(中位9.09 vs. 4.63, P = 0.018)。在发现颅骨转移后的中位随访23.4个月(四分位间距[IQR] 8.7-34.1), 11例激素敏感和所有去势抵抗患者中有5例(45.5%)死于PCa。去势抵抗性疾病患者的中位生存期为9.92个月。结论:大多数PSMA检测到的颅骨转移未显示CT对应,这可能解释了为什么在PSMA pet时代之前很少发现颅骨转移。在高体积转移性前列腺癌病例中,68Ga-PSMA PET/CT成像场(包括顶点)可提高检测肿瘤范围和代谢肿瘤体积的准确性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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